Development Scientist Microbial Cell Bank
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In this job, 425 million people worldwide depend on you to produce, store and maintain cell banks under GMP and thereby contribute to developing the world’s best drugs. If you find challenges like this exciting and inspiring, you may be our new Development Scientist within Microbial Cell Bank production for new treatments.
About the department
The department, Microbial Cell Bank is anchored in CMC API Pilots. CMC API Pilots is a part of the R&D organisation, that manufactures and controls new drug substance candidates for the development portfolio at Novo Nordisk. The department is responsible for producing and maintaining microbial cell banks for clinical trials and marketed products under GMP. We do so in close collaboration with the research unit as well as our quality assurance organisation, regulatory affairs and QC laboratories. The department is located in Bagsværd, Copenhagen, Denmark.
The job
As a Development Cell Bank Scientist your job will be to produce, store and maintain cell banks under GMP together with another scientist and two technicians. You will perform operational work in our laboratory and cell bank facility, but the main part of your job will be handling of documentation. Your tasks include ensuring that, the production, storage and characterisation of our cell banks are in compliance with internal and external quality requirements. As part of the characterisation of cell banks, you will to a lesser extent work with small scale fermentations. You will also handle change requests and actions related to deviations from the cell banking procedures. Because we produce and maintain the inoculation material for all Novo Nordisk products produced by microbial cells, you will be involved in audits and inspections by Health Authorities as well.
We expect you to independently plan, execute and report on assignments while also cooperating closely with your colleagues. In addition, you will be responsible for identifying opportunities for improving processes and compliance.
Qualifications
You have a scientific background with a Master degree or PHD within life science and experience from the pharmaceutical industry combined with:
- a solid knowledge about cellular and molecular biology
- a proven track record within GMP knowledge that enables you to understand what kind of impact changes can have on internal processes and compliance with filed documentation.
- experience with systematic problem-solving
As a person, you:
- have a strong quality mind-set
- are goal oriented and take pride in delivering your task at the right time, in the right quality
- enjoy a working day with very diverse and changing tasks
- have excellent cooperation and communication skills, as your ability to interact with colleagues at various organisational levels is key in achieving success in this position.
Working at Novo Nordisk
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.
Contact
If you have any questions please contact Susan Aagaard on +45 3075 2712
Deadline
19th of October 2019
Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.
Information og data
Denne ledige stilling har jobtypen "Forsker", og befinder sig i kategorien "Sundhed og forskning".
Arbejdsstedet er beliggende i Bagsværd.
Jobbet er oprettet på vores service den 2.10.2019, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Forsker
- Bagsværd
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